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5-(Aminomethyl)-2-ethylpyrimidin-4-amine is an organic compound with the molecular formula C7H11N5. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The presence of an aminomethyl group (-CH2NH2) at the 5-position and an ethyl group (-CH2CH3) at the 2-position distinguishes 5-(AMinoMethyl)-2-ethylpyriMidin-4-aMine from other pyrimidine derivatives. This chemical is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential applications in the treatment of viral infections and cancer. Its unique structure allows for further functionalization and modification, making it a valuable building block in the development of new therapeutic agents.

1886-36-8

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1886-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1886-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1886-36:
(6*1)+(5*8)+(4*8)+(3*6)+(2*3)+(1*6)=108
108 % 10 = 8
So 1886-36-8 is a valid CAS Registry Number.

1886-36-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(aminomethyl)-2-ethylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:1886-36-8 SDS

1886-36-8Relevant academic research and scientific papers

Process for the preparation of a 2-alkyl-4-amino-5-aminomethylpyrimidine

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, (2008/06/13)

There is disclosed a process for the preparation of a 2-alkyl-4-amino-5-aminomethylpyrimidine, which comprises subjecting a 2-alkyl-4-amino-5-formylpyrimidine to catalytic reaction with hydrogen and ammonia in the presence of a reduction catalyst. According to the process of this invention, the desired product can be obtained in much higher yield as compared with the processes known to the art.

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